Issues in CPPD Nomenclature and Classification

Curr Rheumatol Rep. 2019 Jul 25;21(9):49. doi: 10.1007/s11926-019-0847-4.

Abstract

Purpose of review: This paper covers confusion and challenges in the nomenclature of calcium pyrophosphate deposition disease. Clinicians, investigators, and patients are faced with a variety of terms that are used to describe CPPD and its phenotypes, and clarity is greatly needed to help advance research and patient care. Motivation for the upcoming development of CPPD classification criteria is reviewed.

Recent findings: EULAR proposed recommended terminology for CPPD in 2011. International Classification of Diseases (ICD-9 and ICD-10) billing codes identify definite or probable CPPD with variable accuracy depending on the clinical setting and comparator group. READ diagnostic codes have been employed to identify pseudogout in UK datasets but their accuracy has not been evaluated. CPPD classification criteria will provide a system for identifying a relatively homogenous group of patients to be included in clinical studies, enabling comparison of outcomes across studies. CPPD nomenclature remains challenging for clinicians, investigators, and patients. A lay-friendly definition of CPPD, using easily accessible terminology, would be welcome. CPPD classification criteria are a necessary step in moving forward CPPD clinical research and may involve a range of clinical, laboratory, and imaging modalities.

Keywords: Acute CPP crystal arthritis; CPPD; Classification criteria; Nomenclature; Pseudogout; Terminology.

Publication types

  • Review

MeSH terms

  • Calcium Pyrophosphate*
  • Chondrocalcinosis / classification*
  • Chondrocalcinosis / diagnostic imaging
  • Chondrocalcinosis / pathology
  • Humans
  • International Classification of Diseases
  • Terminology as Topic*

Substances

  • Calcium Pyrophosphate